Showing posts with label Discrimination. Show all posts
Showing posts with label Discrimination. Show all posts

Tuesday, November 6, 2012

When Hell Freezes Over. - Day 6 WEGO National Health Blog Month

Day #6 Nov. 6th WEGO National Health Blog Month
Prompt: Write about a time you took the "high road".

If you enjoy my blogs and articles, please nominate me! Only takes a second! CLICK HERE TO NOMINATE ME!!! #HAAwards #NHBPM
 

NOTE: To avoid using curse words, I have used the words "evil witch" in place of... Well, I'm sure it's obvious.
"Girl, you just need to realize that your illness is all in your head. You need to stop feeling sorry for yourself and pretending you are sick with an imaginary disease and just go back to being a human being like me and my son. If you really are sick like you say, you're making yourself sick on your own." says the evil witch.

As the inside of me laughs, thinking of a million words to call this evil witch, I remember that "talking back" or yelling at this evil witch for her rude and pompous speech means that I will only stoop to her unintelligent level. Therefore, I look into the evil witch's eyes, give her a great big smile and say "Have a great day, ma'am." and I walk away with my friends.
 
 
That's right, friends. Hell has frozen over.
 

 
This won't be a long blog. Not tons to say about this situation since I didn't fire back at this evil witch like I wanted to. At a friend's party, speaking with two women there who had Epilepsy. Another woman walks into the area because she overhears us three talking about the side effects we hate, what types of seizures we have, what treatments we use, etc. And this woman feels like she has the right to tell us all that we have a mental illness and that Epilepsy isn't real.
 
My neurons started to fire from all the shock as this evil witch threw insults at the three of us.
 
 
 
 
 
What the hell?
 
How isn't it real?
 
Would it be real if I had a seizure in front of you?
 
Would if be real if your son had Epilepsy?
 
Would it be real if YOU had Epilepsy?
 
Should I get up and tear into you with rude words about your ugly dress?
 
 
When my mind hit the last thought, I realized immediately that I was stooping to this evil witch's level. So I apologized to the good Lord for my terrible thoughts, said something nice, and just walked away with my friends. I took the high road. Avoided a stressful argument that would probably throw me into a seizure. Avoided hurting someone else by making rude comments. But most of all, kept my ground as a respectful young woman in spite of ugly comments. And that alone made me feel good!
 
So, my friends... Take the high road and avoid the crap in life altogether! Evil witches can't hurt you if you just don't care.
 
ALSO - check out the fan pages for tons of cool stuff this month!!! This includes giveaways, cool facts to share with friends, fun Facebook gear to show your advocacy and/or support for others, and much, much more!!! And PLEASE - don't forget to send your awareness month photos to MandyKrzywonski@EpilepsyBlogger.org so you can be on the blog!!!



(EVERYTHING EPILEPSY!)


 
(For mothers, fathers, aunts, uncles,
grandmas, grandpas, nieces, nephews, step-fathers, step-mothers,
daughters, sons, step-daughters, step-sons, friends, best friends,
wives, husbands, couples, and so on! Even singles!!!)

 

(Hopeful words, videos, music, and more to brighten up your day!)

 

Loved ones of those with Epilepsy also welcomed.
Topics posted each week by Mandy (EpilepsyBlogger).
All ages!
 
 
Happy Epilepsy Awareness Month!
EpilepsyBlogger
Mandy Krzywonski

Tuesday, January 24, 2012

Dating... with Epilepsy: Mandy & Rafael - Part One

Rafael and Mandy sharing a dance at Mandy's high school graduation party in June 2011.

   By: Mandy Krzywonski


Introduce you and your boyfriend, Rafael.

You all know me pretty well by now… After all, this is my blog, isn’t it? Anyhow, for those of you who are reading my blog for the very first time, my name is Mandy. I’m 18 years old, and I have had Epilepsy for about 7 years now. If you have Epilepsy, or your loved one has Epilepsy, you don’t need me to tell you that the road of love is extremely rough. (As if it isn't already?) Something about having a loved one with a disability makes things difficult, but it also makes things beautiful in a lot of ways that are extremely overlooked.

Tuesday, November 1, 2011

Meredith's Story - No Longer a Cheerleader, But Still a Leader!

Happy Epilepsy Awareness Month to 
the the U.S.A. and Canada!

Let's kick this month off with a story that touched my heart...






"My name is Meredith,
I'm a freshman in high school, and I have temporal lobe epilepsy. I go to a private school that has now declared that I am not allowed to be on the cheerleading team because of my seizures."